Blood Test Looks at Patients’ Whole Genome to Spot Rare Inherited Diseases
MONDAY, Nov. 8, 2021 (HealthDay News) — Whole genome sequencing of blood samples improves detection of rare genetic conditions called mitochondrial disorders, British researchers report. These disorders are inherited and affect about 1 in 4,300 people, causing progressive, incurable diseases. Though they are among the most common inherited disorders, mitochondrialContinue Reading